Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
  • C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
  • C07C227/18—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
  • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
  • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
  • C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
  • C07C59/235—Saturated compounds containing more than one carboxyl group
  • C07C59/245—Saturated compounds containing more than one carboxyl group containing hydroxy or O-metal groups
  • C07C59/285—Polyhydroxy dicarboxylic acids having five or more carbon atoms, e.g. saccharic acids

Definitions

• the present invention relates to an improved process for preparing stable, non-hygroscopic salts of L(-)carnitine and al anoyl L(- )carnitines .
• compositions which may contain other active ingredients, e.g. with a nutritional and/or dietetic effect.
• compositions which are administered orally constitute by far the most preferable administration form for a vast range of users and are increasingly establishing themselves on the so- called health food, medical food or neutraceutical market.
• These terms which have yet to be rigourously defined from the regulatory point of view, denote foods or food components such as food supplements, dietetic products, energy foods, and the like, i.e.
• formulations which are not addressed to mainly or exclusively therapeutic purposes but which are aimed rather at enhancing well-being and at producing a general improvement in fitness and performance on the part of the consumer or at preventing metabolic disorders caused by dietary deficiencies or by the inadequate biosynthesis of essential endogenous substances as a result of advancing age.
• L( - )carnitine and its derivatives in this field stems from the increasingly widespread recognition, corroborated by scientific evidence, that L(- )carnitine and the lower alkanoyl L(- )carnitines , in addition to their well-known therapeutic value in the treatment of various diseases, make a marked contribution towards supplying energy to the skeletal musculature and increasing the resistance to prolonged, intense stress in professional athletes or in any subject practising sport also at amateur level, enhancing the performance capability of such subjects.
• L( - )carnitine or its lower alkanoyl derivatives constitute indispensable nutritional supplements for vegetarians, whose diets have a low carnitine content as well as a low content of the two amino acids, lysine and methionine, which are the precursors of the biosynthesis of L(- )carnitine in the kidneys and liver.
• L(- )carnitine tablets have to be packaged in blisters to keep them out of contact with the air, since, otherwise, even in the presence of normal humidity conditions, they would undergo alterations, swelling up and becoming pasty and sticky.
• traces of trimethylamine are released which give the products an unpleasant fishy odour.
• the pharmaceutical technologist is indeed interested in having at his disposal salts of L(- )carnitine and its derivatives which, unlike the inner salts, are solid and stable, particularly even in conditions of prolonged storage, which are non- hygroscopic and therefore can be easily processed and formulated with the usual excipients, using blending, tabletting devices, etc., of a traditional type, and which, in addition, pose no packaging problems when converted into finished products.
• These salts, both in the form of raw materials and when formulated in finished products should not, even in non-ideal storage conditions, release traces of trimethylamine which would have a repulsive effect on the user.
• Japanese patent No. 303067 (Tanabe Seiyaku), published on 19.6.1962, publication No. 5199/19, discloses a process for the preparation of carnitine orotate, teaching that it is "advantageously less hygroscopic than carnitine and its typical salt, i.e. carnitine chloride, and can therefore be easily processed" .
• US patent 4,602,039 (Sigma-Tau) granted on 22.7.1986 discloses acid maleate and acid fumarate of L(- )carnitine .
• EP 0434088 discloses the use of the non-hygroscopic L( - )carnitine L( + )tartrate (2:1) (the preparation and physico-chemical characterization of which were however described by D. M ⁇ ller and E. Strack in Hoppe Seyler's Z. Physiol. Chem. 353. 618- 622, April 1972) for the preparation of solid forms suitable for oral administration, such as tablets, capsules, powders or granulates.
• R is hydrogen or lower, straight or branched alkanoyl group having 2-5 carbon atoms; n is 1 or 2;
• X n ⁇ is the monoanion or dianion of a pharmacologically acceptable organic dicarboxylic acid H + X n ⁇ apt to form stable and non-hygroscopic salts with L(-)- carnitine or the alkanoyl L(- )-carnitine; and m is 0; 0.5; 1; 1.5 or 2, comprises :
• step (c) if it is preferred to accelerate the solidification/dehydration of the reaction mixture obtained in step (b), instead of allowing the reaction mixture to stand, a stream of air at a temperature slightly higher than room temperature and low relative humidity can be conveyed over the mixture or the mixture can be fed into a continuous drier or batch drier such as a turbotray drier, direct- heat rotary drier, drum drier, belt drier, spray drier, fluid bed drier and similar industrial driers well known to those skilled in chemical technology (see. e.g. "Drying” in Kirk-Othmer ' s Encyclopedia of Chemical Technology, vol. 8, pages 91-112, 1979).
• a stream of air at a temperature slightly higher than room temperature and low relative humidity can be conveyed over the mixture or the mixture can be fed into a continuous drier or batch drier such as a turbotray drier, direct- heat rotary drier, drum drier, belt drier, spray drier
• the solidification of the reaction mixture can be carried out by treating it with a very small volume of a non-toxic volatile, water-miscible solvent wherein the L( - )carnitine and alkanoyl L( - )carnitine salts are insoluble, such as e.g. acetone.
• a non-toxic volatile, water-miscible solvent wherein the L( - )carnitine and alkanoyl L( - )carnitine salts are insoluble, such as e.g. acetone.
• the process of the present invention is particularly suited for the preparation of the salts of formula (I) wherein, if R is alkanoyl, this is selected from the group comprising acetyl, propionyl, butyryl, valeryl and isovaleryl.
• the organic acid H + n X n ⁇ is preferably selected from the group comprising L( + ) -tartaric, fu aric, mucic and
• salts of formula (I) particularly preferred for preparation via the process of the present invention are: L ( - )-carnitine L ( + )-tartrate (2:1), L(-)- carnitine acid fumarate (1:1), L( - )-carnitine mucate
• L(-)carnitine mucate could be ground to the wanted particle size.
• Example 1 was then followed.
• the reaction mixture behaviour was the same as that of Example 1.
• the water content of the end product [propionyl L(- )carnitine mucate (2:1)] was 5.4- 5.9% by weight.
• the solidification time of the tartrate was longer than that of the mucate, but the times became comparable to each other when an air stream at relative humidity of ten units lower than that used for mucate solidification was blown on the sample.
• the L(- )-carnitine content calculated on the anhydrous product, was 68.2%.
• Example 7 L(-)-carnitine fumarate (1:1) 8.05 g (0.05 moles) of L ( - )-carnitine and 1.5 mL of distilled water were mixed in a mortar giving a semiliquid slurry. 5.80 g (0.05 moles) of fumaric acid were added to the slurry and the resulting mixture was thoroughly blended with a pestle, yielding almost immediately a homogeneous, semitransparent, colourless
• the L( - )-carnitine content calculated on the anhydrous product, was 58.1% by weight.
• the moisture content of the end product depends on many factors such as the moisture content of the starting L(- )carnitine or alkanoyl L ( - )carnitine , the temperature and relative humidity of the air in the plant where the production operations are carried out, the overall processing duration and the particle size of the final product.
• the dehydration time can be shortened by placing the product in an environment of low relative humidity (e.g. 30-40%) and/or by conveying on the product a stream of air of low relative humidity, at room temperature or slightly higher.
• an environment of low relative humidity e.g. 30-40%

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• 1997
  • 1997-02-25 IT IT97MI000409A patent/IT1289974B1/it active IP Right Grant
• 1998
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  • 1998-02-24 HU HU0001674A patent/HUP0001674A3/hu unknown
  • 1998-02-24 JP JP53728998A patent/JP2001513096A/ja not_active Ceased
  • 1998-02-24 AU AU68229/98A patent/AU724276B2/en not_active Ceased
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  • 1998-02-24 DK DK98913582T patent/DK1019362T3/da active
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  • 1998-02-24 EP EP98913582A patent/EP1019362B1/en not_active Expired - Lifetime
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• 1999
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